A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457059



Internal ID22514940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102837296..102838695hg38UCSC Ensembl
chr11:102708027..102709426hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855726
Supporting Variants
Samples
Known GenesMMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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